Taiwan FDA registration c4bcb7f1a412a0e13230b6be655e9eb9

"Simogine" RESI Blood Bank Centrifuge for In Vitro Diagnostics (Unsterilized)

TW: "詩莫吉內" 睿思體外診斷用血庫離心機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·THERMOGENESIS CORPORATION·Registered Mar 12, 2012 – Mar 12, 2017Cancelled
Registration details
Analysis ID
c4bcb7f1a412a0e13230b6be655e9eb9
Customs Code
DHA04401145802
Company information
Manufacturer Country
United States
Product details
Intended Use
Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9275 Blood bank centrifuge for in vitro diagnostics
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Mar 12, 2012
Expiry Date
Mar 12, 2017
Cancellation Date
Nov 15, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Simogine" RESI Blood Bank Centrifuge for In Vitro Diagnostics (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4bcb7f1a412a0e13230b6be655e9eb9 and manufactured by THERMOGENESIS CORPORATION. The authorized representative in Taiwan is Polytechnic Technology Engineering Consultants Limited.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices